Results 81 to 90 of about 1,157,565 (202)

Systemic lupus erythematosus in a 9-year-old patient with beta-thalassemia trait. A case report

, 2015
We reported a case of lupus nephritis in a 9-year-old patient with beta-thalassemia trait who was treated in Cipto Mangunkusumo Hospital. The patient presented with bicytopenia, hepatosplenomegaly and lymphadenopathy.
Ninik Sukartini, Ninik Sukartini
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Discrimination Indices for Diagnosis of Beta(β) Thalassemia Trait [PDF]

, 2018
Background: To determine the reliability ofhematological indices and derived formulas indiagnosing beta thalassemia trait.Methods: In this observational cohort study,patients diagnosed as beta thalassaemia minor wereincluded.
Darakhshan Ahmad , Nadeem Ikram , Shabnum Bashir, Asif Yasin
core   +1 more source

Red Cell Parameters in Beta Thalassemia Trait; Comparison between Iron Deficient and Non-Deficient Carriers

Journal of Bahria University Medical and Dental College
Objective: To compare hematological parameters in iron-deficient and non-deficient carriers of beta thalassemia trait. Study Design And Setting: Comparative cross-sectional study.
Nazish Tahir, Saeed Akhtar Khan Khattak, Ghulam Murtaza Shaikh, Zunera Sajjad, Tamoor Bin Hanif, Nighat Jamal   +5 more
doaj   +1 more source

Talassemia β heterozigotica com triplicação do gene α globínico.

Acta Médica Portuguesa, 2011
We describe a case in which the interaction of heterozygosis for the mutation Beta IVSI - 110 G> A and the ααα(anti 3,7) allele was the likely cause of the clinical occurrence of thalassemia intermedia.
Ma Conceição Constanço, Paula Rocha, Celeste Bento, Helena M Silva   +3 more
doaj   +1 more source

Analysis of thalassemia syndromes and abnormal hemoglobins in patients from the Aegean region of Turkey

The Turkish Journal of Pediatrics, 2002
Turkey is located in a geographic area of the world where thalassemia syndromes and abnormal hemoglobins are common. In this study we aimed to evaluate the thalassemia syndromes and abnormal hemoglobins in patients from the Aegean region of Turkey.
Gülersu Irken, Hale Oren, Bülent Undar, Murat Duman, Hüseyin Gülen, Canan Uçar, Namik Sanli   +6 more
doaj  

A Comparative Study of Liver and Kidney Function Indicators in Patients with Beta-thalassemia Major and Beta-thalassemia Trait [PDF]

Al-Anbar Medical Journal
Background: Comparative analysis of liver and kidney function in patients with beta-thalassemia major (BTM) and beta-thalassemia trait (BTT) is relatively underexplored in the existing literature.Objectives: This study compares liver and kidney function ...
Enaam AL-Dagestani, Mohammad Hamza, Nabaa Yusif   +2 more
doaj   +1 more source

Frequency of beta thalassemia trait and carrier in Gorgan, Iran

, 2010
Objectives: To determine the frequency of beta-Thalassemia trait and carrier in Gorgan, Iran. Methodology: In this analytic cross sectional study conducted from March 20, 2003 until March 20, 2004, two thousands six hundred prospective grooms and brides ...
Vafai, F., Rabie, M.R., Mirbehbahani, N., Jahazi, A.   +3 more
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Role of Discrimination Indices in Screening of Beta Thalassemia Trait in Low-Resourced Areas of Pakistan

, 2020
: Introduction: Thalassemia is a common inherited hemoglobinopathy in Pakistan. Despite various preventive measures taken, each year around 5000 new cases are diagnosed. The problem occurs due to undiagnosed beta Thalassemia carriers.
Zulfiqar, Maryam, Ali, Bushra Anam, Mustafa, Asma, Naseem, Lubna   +3 more
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Diagnostic test performance of the Mentzer index in evaluating Saudi children with microcytosis

Frontiers in Medicine
BackgroundAnemia is a global public health concern, affecting both developing and industrialized countries at a rate of 39.8%. It is defined by low hemoglobin concentration, and anemia varies in severity based on age: <11 g/dL (6–59 months), <11.5 ...
Amani M. AlQarni, Arwa Althumairi, Nourah K. Alkaltham, Samaa AlJishi, Amani Mohammed Hakami, Leena Mohamed Osman Ali Abdalla, Leena Mohamed Osman Ali Abdalla, Zahra Sayed Jalal Alawi, Zahra Sayed Jalal Alawi, Abdullah H. Alreedy   +9 more
doaj   +1 more source

Evaluation of Abnormal Hemoglobin Variants and Hemoglobinopathies on D-10 Analyzer – An Institutional Experience from North India.

Online Journal of Health & Allied Sciences, 2022
Background: High performance liquid chromatography (HPLC) is the most commonly used method for detection and quantitative estimation of hemoglobin variants.
Shivali Sehgal, Sabina Khan, Sujata Jetley, Yasir Alvi   +3 more
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